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Last Updated: 3 years ago

Possible Interaction: Oxytocin and Ng-Nitroarginine Methyl Ester

Research Papers that Mention the Interaction

In the presence of L-NAME , plasma AVP and OT levels rose 3-fold in response to hypoglycemia and were significantly higher than those in the control test.
Regulatory Peptides  •  1996  |  View Paper
Since oxytocin's effects during the early phase were also antagonized by Nω-nitro-l-arginine methyl ester , ODQ, or glibenclamide (inhibitors of nitric oxide synthase [NOS], soluble guanylyl cyclase [GC], and K+ATP channels, respectively), the role of two differential pathways elicited by oxytocin is supported.
ACS chemical neuroscience  •  2021  |  View Paper
In addition, administration of l-NAME prior to OT partially reversed the protective effect of OT ensuring that one of the protective effects of OT was through the NO production.
Journal of basic and clinical physiology and pharmacology  •  2017  |  View Paper
The ANP receptor antagonist (anantin) and NO synthases inhibitor l-NAME ) inhibited cGMP production in CMs exposed to OT.
International journal of cardiology  •  2014  |  View Paper
In L-NAME + MgSO4 given group at each oxytocin concentrations, the frequencies of the contractions in ten-min period were lower but not statistically different than the L-NAME group.
Clinical and experimental obstetrics & gynecology  •  2014  |  View Paper
Pretreatment of L-NAME (10 mmol/L, 100 nl), the nitric oxide synthase (NOS) inhibitor, or methyl blue (10 mmol/L, 100 nl), the guanylyl cyclase inhibitor, inhibited the excitatory effect of OT on gallbladder motility.
Brain Research  •  2005  |  View Paper
The effects of OT were also blocked by hexamethonium, a ganglionic blocking agent, by atropine, a muscarinic receptor antagonist, and by N(omega)-nitro-L-arginine methyl ester , an inhibitor of nitric oxide synthesis.
American journal of physiology. Regulatory, integrative and comparative physiology  •  2005  |  View Paper
Treatment of morphine‐dependent rats with Nω‐nitro‐l‐arginine methyl ester also enhanced oxytocin secretion during naloxone‐precipitated withdrawal.
The European journal of neuroscience  •  2003  |  View Paper
Co-perfusion with 10−… NO synthase inhibitor L-NAME) … oxytocin effects on both beating rate (−1.85±1.27% versus −14.7±4.9% in oxytocin alone, P <0.05) … of contraction (−24.9±4.4% versus −52.4±9.1% in oxytocin alone, n=4, P <0.04).
The effect of oxytocin on contractility was further inhibited by L-NAME at 10−4 mol/L (−8.1±1.8%, P <0.01).
Hypertension  •  2001  |  View Paper
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